MAKITA Yoshio

J-GLOBAL         Last updated: Oct 15, 2018 at 10:03
 
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Name
MAKITA Yoshio
Affiliation
Asahikawa Medical College
Section
School of Medicine, Education Center
Job title
Professor
Degree
(BLANK)(Asahikawa Medical College)

Research Areas

 
 

Education

 
 
 - 
1991
Graduate School, Division of Medicine, Asahikawa Medical College
 
 
 - 
1987
Faculty of Medicine, Asahikawa Medical College
 

Published Papers

 
Genitopatellar syndrome: the first reported case in Japan.
Okano S, Miyamoto A, Fukuda I, Tanaka H, Hata K, Kaname T, Matsubara Y, Makita Y.
Hum Genome Var.   28(5) 8-8   May 2018   [Refereed]
Genomic Characterization of chromosomal insertions: Insight into the mechanisms underlying chromothipsis
Kato T, Ouchi Y, Inagaki H, Makita Y, Mizuno S, Kajita M, Ikeda T, Takeuchi K, Kurahashi H.
Cytogenet Genome Res.   153(1) 1-9   Jan 2017   [Refereed]
Uehara DT Hayashi S, Okamoto N, Mizuno S, Chinen Y, Kosaki R, Kosho T, Kurosawa K, Matsumoto H, Mitsubuchi H, Numabe H, Saitoh S, Makita Y, Hata A, Imoto I, Inazawa J.
J Hum Genet.   61(4) 335-343   Apr 2016   [Refereed]
Miyatake S, Koshimizu E, Fujita A, Fukai R, Imagawa E, Ohba C, Kuki I, Nukui M, Araki A, Makita Y, Ogata T, Nakashima M, Tsurusaki Y, Miyake N, Saitsu H, Matsumoto N.
J Hum Genet.   60(4) 175-182   Apr 2015   [Refereed]
Maeda T, Higashimoto K, Jozaki K, Yatsuki H, Nakabayashi K, Makita Y, Tonoki H, Okamoto N, Takada F, Ohashi H, Migita M, Kosaki R, Matsubara K, Ogata T, Matsuo M, Hamasaki Y, Ohtsuka Y, Nishioka K, Joh K, Mukai T, Hata K, Soejima H.
Genet Med.   16(12) 903-912   Dec 2014   [Refereed]

Research Grants & Projects

 
Ministry of Education, Culture, Sports, Science and Technology: Grants-in-Aid for Scientific Research(基盤研究(B))
Project Year: 2008 - 2010    Investigator(s): Yoshio MAKITA
We developed a diagnostic array(Genome Disorder Array) in order to exclude structural chromosome aberrations in patients with known chromosomal micro-deletion and micro-duplication syndromes. Genome Disorder Array version 3.0 was selected to deter...
Isolation of responsible genes, involving multiple congenital anomalies, using CGH-microarray method
Cooperative Research
Project Year: 2005 - 2010
Ministry of Education, Culture, Sports, Science and Technology: Grants-in-Aid for Scientific Research(基盤研究(C))
Project Year: 2003 - 2005    Investigator(s): Yoshio MAKITA
[Background] Rapid proceeding of human genome project, we got many knowledge for genetic defects of simple mendelian diseases. But simple mendelian diseases were rare diseases ; frequency was 1.25% of born infants. Now our interest goes toward com...